NKX2-6 Antibody

Code CSB-PA003457
Size US$119
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  • Western Blot analysis of COLO205 cells using Nkx-2.6 Polyclonal Antibody
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Product Details

Uniprot No.
Target Names
NKX2-6
Alternative Names
NKX2-6 antibody; NKX2F antibody; Homeobox protein Nkx-2.6 antibody; Homeobox protein NK-2 homolog F antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Synthesized peptide derived from the Internal region of Human Nkx-2.6.
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Isotype
IgG
Purification Method
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Form
Liquid
Tested Applications
WB, ELISA
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:2000
ELISA 1:40000
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Acts as a transcriptional activator. In conjunction with NKX2-5, may play a role in both pharyngeal and cardiac embryonic development.
Gene References into Functions
  1. This study firstly links NKX2.6 loss-of-function mutation with increased susceptibility to isolated VSD. PMID: 25380965
  2. Data associated genetically defective NK2 homeobox 6 (NKX2-6) with enhanced susceptibility to atrial fibrillation (AF). PMID: 25319568
  3. Heterozygous mutations in Nkx2.6, p.V176M and p.K177X, were identified in 2 unrelated patients, one with tetralogy of Fallot and one with double outlet of right ventricle and ventricular septal defect. Increased vulnerability to TOF or DORV is discussed. PMID: 25195019
  4. NKX2-6 plays a role in human cardiogenesis. PMID: 24421281
  5. weakly activates transcription of a Cx40 promoter, may have role in heart development PMID: 15649947
  6. NKX2.5/NKX2.6 mutations are not a common cause of isolated type 1 truncus arteriosus in a small cohort of multiethnic cases. PMID: 18939937

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Involvement in disease
Conotruncal heart malformations (CTHM)
Subcellular Location
Nucleus.
Protein Families
NK-2 homeobox family
Database Links

HGNC: 32940

OMIM: 217095

KEGG: hsa:137814

STRING: 9606.ENSP00000320089

UniGene: Hs.532654

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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